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T81604

Sigma-Aldrich

Triphenylamine

98%

Synonim(y):

N,N-Diphenylaniline, N,N-Diphenylbenzenamine

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About This Item

Wzór liniowy:
(C6H5)3N
Numer CAS:
603-34-9
Masa cząsteczkowa:
245.32
Beilstein:
2050487
Numer WE:
210-035-5
Numer MDL:
MFCD00003020
Kod UNSPSC:
12352100
Identyfikator substancji w PubChem:
24900507
NACRES:
NA.22

Próba

98%

tw

347-348 °C (lit.)

mp

124-128 °C (lit.)

ciąg SMILES

c1ccc(cc1)N(c2ccccc2)c3ccccc3

InChI

1S/C18H15N/c1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15H

Klucz InChI

ODHXBMXNKOYIBV-UHFFFAOYSA-N

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Zastosowanie


  • Photoinitiators for Hydrogel Formation: Triphenylamine derivatives are used as novel D-pi-A hemicyanine dyes, acting as effective photoinitiators for in situ hydrogel formation and DLP printing, expanding their applications in biomedical engineering and 3D printing technologies (Du et al., 2024).

  • Supramolecular Photosensitizers: A supramolecular construct based on triphenylamine and pyrazine demonstrates aggregation-induced emission properties, enhancing the efficiency of photooxidation reactions. This development offers potential improvements in photodynamic therapy and environmental applications (Dong et al., 2024).

  • Highly Efficient OLEDs: Triphenylamine is integral in synthesizing new phenanthro[9,10-d]oxazole-based fluorophores with hybridized local and charge-transfer characteristics. These materials are crucial for developing blue non-doped OLEDs with minimal efficiency roll-off, significant for advanced display technologies (Xie et al., 2024).

  • Memory Device Applications: Modifications in donor end caps in N-heteroaromatic systems containing triphenylamine were explored for binary-to-ternary WORM memory conversion, contributing to advancements in memory storage technology (Gayathri et al., 2024).

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Kod klasy składowania

11 - Combustible Solids

Klasa zagrożenia wodnego (WGK)

WGK 2

Temperatura zapłonu (°F)

Not applicable

Temperatura zapłonu (°C)

Not applicable

Środki ochrony indywidualnej

dust mask type N95 (US), Eyeshields, Gloves

Certyfikaty analizy (CoA)

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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

Jiu-Qiang Huang et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 154, 164-170 (2015-11-02)
A new series of trans-alkenes (3a-3e) containing different electron-donating groups were synthesized by the solvent-free Horner-Wadsworth-Emmons reaction, and characterized by infrared, hydrogen nuclear magnetic resonance, mass spectrometry and elemental analysis. Their UV-visible absorption, one-photon excited fluorescence, two-photon absorption, and two-photon
Minggang Tian et al.
Organic & biomolecular chemistry, 12(32), 6128-6133 (2014-07-06)
Cysteine (Cys) plays important roles in many physiological processes of eukaryotic cells and its detection in cells is of fundamental significance. However, glutathione (GSH), homocysteine, N-acetyl-L-cysteine and other thiols greatly hamper the detection of Cys. In particular, GSH strongly interferes
Xu Jing et al.
Journal of the American Chemical Society, 137(11), 3967-3974 (2015-03-05)
The design of artificial systems that mimic highly evolved and finely tuned natural photosynthetic systems is a subject of intensive research. We report herein a new approach to constructing supramolecular systems for the photocatalytic generation of hydrogen from water by

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